APIE JULLIENO ATSAKYMĄ Į BILLETERIO KRITIKĄ: IŠĖJIMAS ANAPUS KARTEZIŠKOJO COGITO KAIP METODOLOGINIS INTERESAS by Francesco Carpanini

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Leon Battista Alberti / by 404769 Borsi, Franco, Carpanini, Rudolf G.

Leon Battista Alberti : the complete works / by 404769 Borsi, Franco, Carpanini, Rudolf G.

Pitting in soft aluminium produced by spark-induced cavitation bubbles / by 429211 Lush, P. A., Wood, R. J. K., Carpanini, L. J.

Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System by Sarah M. Carpanini, Megan Torvell, Bryan Paul Morgan, Bryan Paul Morgan

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Rab18 and a Rab18 GEF complex are required for normal ER structure. by Gerondopoulos, A, Bastos, R, Yoshimura, S, Anderson, R, Carpanini, S, Aligianis, I, Handley, M, Barr, F

Genetic Insights into the Impact of Complement in Alzheimer’s Disease by Megan Torvell, Sarah M. Carpanini, Nikoleta Daskoulidou, Robert A. J. Byrne, Rebecca Sims, B. Paul Morgan

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The Impact of Complement Genes on the Risk of Late-Onset Alzheimer’s Disease by Sarah M. Carpanini, Janet C. Harwood, Emily Baker, Megan Torvell, The GERAD1 Consortium, Rebecca Sims, Julie Williams, B. Paul Morgan

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Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation by Mark T. Handley, Sarah M. Carpanini, Girish R. Mali, Duska J. Sidjanin, Irene A. Aligianis, Ian J. Jackson, David R. FitzPatrick

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Alzheimer’s disease-associated complement gene variants influence plasma complement protein levels by Aurora Veteleanu, Joshua Stevenson-Hoare, Samuel Keat, Nikoleta Daskoulidou, Henrik Zetterberg, Amanda Heslegrave, Valentina Escott-Price, Julie Williams, Rebecca Sims, Wioleta M. Zelek, Sarah M. Carpanini, Bryan Paul Morgan

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Terminal complement pathway activation drives synaptic loss in Alzheimer’s disease models by Sarah M. Carpanini, Megan Torvell, Ryan J. Bevan, Robert A. J. Byrne, Nikoleta Daskoulidou, Takashi Saito, Takaomi C. Saido, Philip R. Taylor, Timothy R. Hughes, Wioleta M. Zelek, B. Paul Morgan

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A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton by Sarah M. Carpanini, Lisa McKie, Derek Thomson, Ann K. Wright, Sarah L. Gordon, Sarah L. Roche, Mark T. Handley, Harris Morrison, David Brownstein, Thomas M. Wishart, Michael A. Cousin, Thomas H. Gillingwater, Irene A. Aligianis, Ian J. Jackson

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Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1 by Jamie McQueen, Tomás J Ryan, Sean McKay, Katie Marwick, Paul Baxter, Sarah M Carpanini, Thomas M Wishart, Thomas H Gillingwater, Jean C Manson, David J A Wyllie, Seth G N Grant, Barry W McColl, Noboru H Komiyama, Giles E Hardingham

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Loss-of-function mutations in TBC1d20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans by Liegel, R, Handley, M, Ronchetti, A, Brown, S, Langemeyer, L, Linford, A, Chang, B, Morris-Rosendahl, D, Carpanini, S, Posmyk, R, Harthill, V, Sheridan, E, Abdel-Salam, G, Terhal, P, Faravelli, F, Accorsi, P, Giordano, L, Pinelli, L, Hartmann, B, Ebert, A, Barr, F, Aligianis, I, Sidjanin, D